Rapamycin passes the torch: a new generation of mTOR inhibitors

被引:816
作者
Benjamin, Don [1 ]
Colombi, Marco [1 ]
Moroni, Christoph [1 ]
Hall, Michael N. [1 ]
机构
[1] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
P70; S6; KINASE; SENSITIVE PHOSPHOPROTEOME REVEALS; TUBEROUS SCLEROSIS COMPLEX; REDUCES TUMOR-GROWTH; MAMMALIAN TARGET; CELL-GROWTH; LIFE-SPAN; ANTITUMOR-ACTIVITY; PALOMID; 529; 3-KINASE/MAMMALIAN TARGET;
D O I
10.1038/nrd3531
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mammalian target of rapamycin (mTOR) is an atypical protein kinase that controls growth and metabolism in response to nutrients, growth factors and cellular energy levels, and it is frequently dysregulated in cancer and metabolic disorders. Rapamycin is an allosteric inhibitor of mTOR, and was approved as an immunosuppressant in 1999. In recent years, interest has focused on its potential as an anticancer drug. However, the performance of rapamycin and its analogues (rapalogues) has been undistinguished despite isolated successes in subsets of cancer, suggesting that the full therapeutic potential of targeting mTOR has yet to be exploited. A new generation of ATP-competitive inhibitors that directly target the mTOR catalytic site display potent and comprehensive mTOR inhibition and are in early clinical trials.
引用
收藏
页码:868 / 880
页数:13
相关论文
共 163 条
[51]   Rictor/mTORC2 Is Essential for Maintaining a Balance Between β-Cell Proliferation and Cell Size [J].
Gu, Yanyun ;
Lindner, Jill ;
Kumar, Anil ;
Yuan, Weiping ;
Magnuson, Mark A. .
DIABETES, 2011, 60 (03) :827-837
[52]   mTOR Complex 2 Is Required for the Development of Prostate Cancer Induced by Pten Loss in Mice [J].
Guertin, David A. ;
Stevens, Deanna M. ;
Saitoh, Maki ;
Kinkel, Stephanie ;
Crosby, Katherine ;
Sheen, Joon-Ho ;
Mullholland, David J. ;
Magnuson, Mark A. ;
Wu, Hong ;
Sabatini, David M. .
CANCER CELL, 2009, 15 (02) :148-159
[53]   AMPK phosphorylation of raptor mediates a metabolic checkpoint [J].
Gwinn, Dana M. ;
Shackelford, David B. ;
Egan, Daniel F. ;
Mihaylova, Maria M. ;
Mery, Annabelle ;
Vasquez, Debbie S. ;
Turk, Benjamin E. ;
Shaw, Reuben J. .
MOLECULAR CELL, 2008, 30 (02) :214-226
[54]   Regulation of eIF-4E BP1 phosphorylation by mTOR [J].
Hara, K ;
Yonezawa, K ;
Kozlowski, MT ;
Sugimoto, T ;
Andrabi, K ;
Weng, QP ;
Kasuga, M ;
Nishimoto, I ;
Avruch, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26457-26463
[55]   Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action [J].
Hara, K ;
Maruki, Y ;
Long, XM ;
Yoshino, K ;
Oshiro, N ;
Hidayat, S ;
Tokunaga, C ;
Avruch, J ;
Yonezawa, K .
CELL, 2002, 110 (02) :177-189
[56]   Amino acid sufficiency and mTOR regulate p70 S6 kinase and eIF-4E BP1 through a common effector mechanism [J].
Hara, K ;
Yonezawa, K ;
Weng, QP ;
Kozlowski, MT ;
Belham, C ;
Avruch, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14484-14494
[57]  
Harrington L. S, 2004, J CELL BIOL, V166, P213
[58]   Rapamycin fed late in life extends lifespan in genetically heterogeneous mice [J].
Harrison, David E. ;
Strong, Randy ;
Sharp, Zelton Dave ;
Nelson, James F. ;
Astle, Clinton M. ;
Flurkey, Kevin ;
Nadon, Nancy L. ;
Wilkinson, J. Erby ;
Frenkel, Krystyna ;
Carter, Christy S. ;
Pahor, Marco ;
Javors, Martin A. ;
Fernandez, Elizabeth ;
Miller, Richard A. .
NATURE, 2009, 460 (7253) :392-U108
[59]   TARGETS FOR CELL-CYCLE ARREST BY THE IMMUNOSUPPRESSANT RAPAMYCIN IN YEAST [J].
HEITMAN, J ;
MOVVA, NR ;
HALL, MN .
SCIENCE, 1991, 253 (5022) :905-909
[60]   Phase III Study to Evaluate Temsirolimus Compared With Investigator's Choice Therapy for the Treatment of Relapsed or Refractory Mantle Cell Lymphoma [J].
Hess, Georg ;
Herbrecht, Raoul ;
Romaguera, Jorge ;
Verhoef, Gregor ;
Crump, Michael ;
Gisselbrecht, Christian ;
Laurell, Anna ;
Offner, Fritz ;
Strahs, Andrew ;
Berkenblit, Anna ;
Hanushevsky, Orysia ;
Clancy, Jill ;
Hewes, Becker ;
Moore, Laurence ;
Coiffier, Bertrand .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (23) :3822-3829